CN103992765B - A kind of macromolecule memory material and preparation method thereof - Google Patents
A kind of macromolecule memory material and preparation method thereof Download PDFInfo
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- CN103992765B CN103992765B CN201410254409.6A CN201410254409A CN103992765B CN 103992765 B CN103992765 B CN 103992765B CN 201410254409 A CN201410254409 A CN 201410254409A CN 103992765 B CN103992765 B CN 103992765B
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- memory material
- vacuumizing
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- 239000000463 material Substances 0.000 title claims abstract description 37
- 229920002521 macromolecule Polymers 0.000 title claims abstract description 23
- 238000002360 preparation method Methods 0.000 title claims abstract description 23
- 239000000853 adhesive Substances 0.000 claims abstract description 43
- 230000001070 adhesive effect Effects 0.000 claims abstract description 43
- 238000001035 drying Methods 0.000 claims abstract description 26
- 239000000203 mixture Substances 0.000 claims abstract description 16
- FLKPEMZONWLCSK-UHFFFAOYSA-N diethyl phthalate Chemical compound CCOC(=O)C1=CC=CC=C1C(=O)OCC FLKPEMZONWLCSK-UHFFFAOYSA-N 0.000 claims abstract description 14
- 239000002253 acid Substances 0.000 claims abstract description 9
- VTYYLEPIZMXCLO-UHFFFAOYSA-L calcium carbonate Substances [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 claims abstract description 9
- TXAMMAGYRNMFNW-UHFFFAOYSA-N NN.C1=CC=CC=C1.[S] Chemical compound NN.C1=CC=CC=C1.[S] TXAMMAGYRNMFNW-UHFFFAOYSA-N 0.000 claims abstract description 8
- 238000005119 centrifugation Methods 0.000 claims abstract description 8
- 239000008187 granular material Substances 0.000 claims abstract description 8
- VLTOSDJJTWPWLS-UHFFFAOYSA-N pent-2-ynal Chemical compound CCC#CC=O VLTOSDJJTWPWLS-UHFFFAOYSA-N 0.000 claims abstract description 8
- 229920002742 polystyrene-block-poly(ethylene/propylene) -block-polystyrene Polymers 0.000 claims abstract description 8
- 239000011347 resin Substances 0.000 claims abstract description 8
- 229920005989 resin Polymers 0.000 claims abstract description 8
- 150000003505 terpenes Chemical class 0.000 claims abstract description 8
- 235000007586 terpenes Nutrition 0.000 claims abstract description 8
- 229920002725 thermoplastic elastomer Polymers 0.000 claims abstract description 8
- 229910000019 calcium carbonate Inorganic materials 0.000 claims abstract description 7
- 238000000034 method Methods 0.000 claims abstract description 7
- 229920001971 elastomer Polymers 0.000 claims abstract description 6
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 claims abstract description 5
- 229910021502 aluminium hydroxide Inorganic materials 0.000 claims abstract description 5
- 229920001195 polyisoprene Polymers 0.000 claims abstract description 4
- 229910052782 aluminium Inorganic materials 0.000 claims description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 claims description 2
- UHOVQNZJYSORNB-UHFFFAOYSA-N monobenzene Natural products C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 1
- 239000011575 calcium Substances 0.000 claims 1
- 229910052791 calcium Inorganic materials 0.000 claims 1
- 229910052799 carbon Inorganic materials 0.000 claims 1
- 229920003244 diene elastomer Polymers 0.000 claims 1
- 125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 claims 1
- 239000002105 nanoparticle Substances 0.000 claims 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 1
- UTGQNNCQYDRXCH-UHFFFAOYSA-N N,N'-diphenyl-1,4-phenylenediamine Chemical compound C=1C=C(NC=2C=CC=CC=2)C=CC=1NC1=CC=CC=C1 UTGQNNCQYDRXCH-UHFFFAOYSA-N 0.000 abstract 1
- -1 dimethyl ethylamino ethylene glycol Chemical compound 0.000 abstract 1
- 230000008901 benefit Effects 0.000 description 4
- PNEYBMLMFCGWSK-UHFFFAOYSA-N Alumina Chemical compound [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- PMJHHCWVYXUKFD-SNAWJCMRSA-N (E)-1,3-pentadiene Chemical compound C\C=C\C=C PMJHHCWVYXUKFD-SNAWJCMRSA-N 0.000 description 2
- 241000209094 Oryza Species 0.000 description 2
- 235000007164 Oryza sativa Nutrition 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 235000009566 rice Nutrition 0.000 description 2
- WWWTWPXKLJTKPM-UHFFFAOYSA-N 2-aminooxyethanol Chemical compound NOCCO WWWTWPXKLJTKPM-UHFFFAOYSA-N 0.000 description 1
- 239000004836 Glue Stick Substances 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229920003049 isoprene rubber Polymers 0.000 description 1
- 238000007711 solidification Methods 0.000 description 1
- 230000008023 solidification Effects 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
Landscapes
- Adhesives Or Adhesive Processes (AREA)
- Tires In General (AREA)
Abstract
The present invention relates to a kind of macromolecule memory material and preparation method thereof, comprise the steps: adhesive paste preparation process, by pentalyn, terpene resin, diethyl phthalate, N, N ' diphenyl-para-phenylene diamine, aluminium hydroxide, nano-calcium carbonate, 4,4 ' bis oxide benzene sulfur hydrazine and N, N dimethyl ethylamino ethylene glycol is fully ground, and hydrolyze under acid or alkaline conditions, add SEPS thermoplastic elastomer and polyisoprene rubber, it is heated to more than its fusing point, mix and blend, until being visible by naked eyes granule, forms adhesive paste;High speed rotating centrifugation step, puts into centrifuge after described adhesive paste is cooled to room temperature, high speed rotating is centrifuged;Vacuumizing and drying step, processes the adhesive paste vacuumizing and drying after centrifugal;Curing schedule, takes out the adhesive paste after centrifugal drying, solidifies the sub-memory material that i.e. secures satisfactory grades for 24 hours at ambient temperature.
Description
Technical field
The present invention relates to a kind of macromolecule memory material and preparation method thereof.
Background technology
Along with consumer is more and more higher for the requirement of automobile tyre security energy, various safety tread occurs.
Therefore produce therewith by reaching technology explosion-proof, leakproof, even bulletproof effect at inside tires spray on polymer layer,
But the polymer leakage-proof mending material intermolecular distance occurred in the market is big, and its adhesive force being attached to internal face is little, long
Still there will be the phenomenon of gas leakage after time use, affect traffic safety, it is therefore desirable to a kind of leakage-proof mending material solves this
One problem.
Summary of the invention
The technical problem to be solved is to provide that a kind of intermolecular distance is little, adhesive ability is strong, may be used for wheel
Macromolecule memory material of tire leakage-proof mending and preparation method thereof.
The preparation method of a kind of macromolecule memory material, it is characterised in that comprise the steps:
Adhesive paste preparation process, by the pentalyn of 30 to 50 parts of weight, the terpene resin of 40 to 50 parts of weight, 10
To the diethyl phthalate of 20 parts of weight, the N of 2 to 5 parts of weight, N '-diphenyl-para-phenylene diamine, the hydrogen of 5 to 10 parts of weight
Aluminium oxide, the nano-calcium carbonate of 5 to 10 parts of weight, 4,4 '-bis oxide benzene sulfur hydrazine of 1 to 5 part of weight and 1 to 3 part of weight
N, N-dimethyl ethylamino ethylene glycol be fully ground, and hydrolyze under acid or alkaline conditions, add 50 to 70 parts of weight
SEPS thermoplastic elastomer and the polyisoprene rubber of 40 to 50 parts of weight, be heated to more than its fusing point, mix and blend is straight
To being visible by naked eyes granule, it is thus achieved that adhesive paste;
High speed rotating centrifugation step, puts into centrifuge after described adhesive paste is cooled to room temperature, high speed rotating is centrifuged 90-120
Minute, rotating speed is 25000 × g-30000 × g;
Vacuumizing and drying step, puts into place in the vacuumizing and drying device that vacuum is 1 Pascal by the adhesive paste after centrifugal
Manage 35-55 minute;
Curing schedule, takes out the adhesive paste after centrifugal drying, solidifies the sub-memory material that i.e. secures satisfactory grades for 24 hours at ambient temperature
Material.
Preferably, in described adhesive paste preparation process, by the pentalyn of 43 parts of weight, the terpenes of 47 parts of weight
Resin, the diethyl phthalate of 16 parts of weight, the N of 3 parts of weight, N '-diphenyl-para-phenylene diamine, the hydroxide of 7 parts of weight
Aluminum, the nano-calcium carbonate of 8 parts of weight, 4,4 '-bis oxide benzene sulfur hydrazine of 2 parts of weight and the N of 2 parts of weight, N-dimethyl second
2-aminooxyethanol is fully ground, and hydrolyzes under acid or alkaline conditions, add 62 parts of weight SEPS thermoplastic elastomer and
The polyisoprene rubber of 45 parts of weight, is heated to more than its fusing point, and mix and blend is until being visible by naked eyes granule, it is thus achieved that glue
Stick with paste;In described high speed rotating centrifugation step, putting into centrifuge after described adhesive paste is cooled to room temperature, high speed rotating is centrifuged 105
Minute, rotating speed is 27500 × g;In described vacuumizing and drying step, it is 1 Pascal that the adhesive paste after being centrifuged puts into vacuum
Vacuumizing and drying device in process 45 minutes;In described curing schedule, take out the adhesive paste after centrifugal drying, at room temperature condition
Lower solidification i.e. secures satisfactory grades sub-memory material for 24 hours.
Accordingly, the present invention also provides for a kind of macromolecule memory material, takes the preparation of described macromolecule memory material
Method makes.
Compared with prior art, the advantage of technique scheme is, it is provided that a kind of intermolecular distance is little, adhesive ability is strong
, may be used for macromolecule memory material of the close benefit of tire leakproof and preparation method thereof.Especially following some obtain prominent
Effect: 1, have employed the mode that high speed rotating is centrifugal, find which can be by macromolecule memory material through Experimental comparison
Molecule be centrifuged dispersion, the distance between reduction molecule, make macromolecule memory material reach nanoscale, and then improve it and inhale
Attached ability.
2, use vacuumizing and drying step, dry under vacuum conditions, can more preferable stable molecule spacing, it is ensured that
The absorbability of macromolecule memory material.
Detailed description of the invention
Below in conjunction with embodiment, the present invention is described further.
Embodiment one:
The preparation method of a kind of macromolecule memory material, it is characterised in that comprise the steps:
Adhesive paste preparation process, by the pentalyn of 30 parts of weight, the terpene resin of 40 parts of weight, 10 parts of weight
Diethyl phthalate, the N of 2 parts of weight, N '-diphenyl-para-phenylene diamine, the aluminium hydroxide of 5 parts of weight, the receiving of 5 parts of weight
Rice calcium carbonate, 4,4 '-bis oxide benzene sulfur hydrazine of 1 part of weight and the N of 1 part of weight, N-dimethyl ethylamino ethylene glycol is abundant
Grind, and hydrolyze under acid or alkaline conditions, add the SEPS thermoplastic elastomer of 50 parts of weight and the poly-different of 40 parts of weight
Pentadiene rubber, is heated to more than its fusing point, and mix and blend is until being visible by naked eyes granule, it is thus achieved that adhesive paste;
High speed rotating centrifugation step, puts into centrifuge after described adhesive paste is cooled to room temperature, high speed rotating is centrifuged 90 minutes,
Rotating speed is 25000 × g;
Vacuumizing and drying step, puts into place in the vacuumizing and drying device that vacuum is 1 Pascal by the adhesive paste after centrifugal
Manage 35 minutes;
Curing schedule, takes out the adhesive paste after centrifugal drying, solidifies the sub-memory material that i.e. secures satisfactory grades for 24 hours at ambient temperature
Material.
Embodiment two:
The preparation method of a kind of macromolecule memory material, it is characterised in that comprise the steps:
Adhesive paste preparation process, by the pentalyn of 43 parts of weight, the terpene resin of 47 parts of weight, 16 parts of weight
Diethyl phthalate, the N of 3 parts of weight, N '-diphenyl-para-phenylene diamine, the aluminium hydroxide of 7 parts of weight, the receiving of 8 parts of weight
Rice calcium carbonate, 4,4 '-bis oxide benzene sulfur hydrazine of 2 parts of weight and the N of 2 parts of weight, N-dimethyl ethylamino ethylene glycol is abundant
Grind, and hydrolyze under acid or alkaline conditions, add the SEPS thermoplastic elastomer of 62 parts of weight and the poly-different of 45 parts of weight
Pentadiene rubber, is heated to more than its fusing point, and mix and blend is until being visible by naked eyes granule, it is thus achieved that adhesive paste;
High speed rotating centrifugation step, puts into centrifuge after described adhesive paste is cooled to room temperature, high speed rotating is centrifuged 105 points
Clock, rotating speed is 27500 × g;
Vacuumizing and drying step, puts into place in the vacuumizing and drying device that vacuum is 1 Pascal by the adhesive paste after centrifugal
Manage 45 minutes;
Curing schedule, takes out the adhesive paste after centrifugal drying, solidifies the sub-memory material that i.e. secures satisfactory grades for 24 hours at ambient temperature
Material.
Embodiment three:
The preparation method of a kind of macromolecule memory material, it is characterised in that comprise the steps:
Adhesive paste preparation process, by the pentalyn of 50 parts of weight, the terpene resin of 50 parts of weight, 20 parts of weight
Diethyl phthalate, the N of 5 parts of weight, N '-diphenyl-para-phenylene diamine, the aluminium hydroxide of 10 parts of weight, 10 parts of weight
Nano-calcium carbonate, 4,4 '-bis oxide benzene sulfur hydrazine of 5 parts of weight and the N of 3 parts of weight, N-dimethyl ethylamino ethylene glycol fill
Divide and grind, and hydrolyze under acid or alkaline conditions, add the SEPS thermoplastic elastomer of 70 parts of weight and the poly-of 50 parts of weight
Isoprene rubber, is heated to more than its fusing point, and mix and blend is until being visible by naked eyes granule, it is thus achieved that adhesive paste;
High speed rotating centrifugation step, puts into centrifuge after described adhesive paste is cooled to room temperature, high speed rotating is centrifuged 120 points
Clock, rotating speed is 30000 × g;
Vacuumizing and drying step, puts into place in the vacuumizing and drying device that vacuum is 1 Pascal by the adhesive paste after centrifugal
Manage 55 minutes;
Curing schedule, takes out the adhesive paste after centrifugal drying, solidifies the sub-memory material that i.e. secures satisfactory grades for 24 hours at ambient temperature
Material.
Compared with prior art, the advantage of technique scheme is, it is provided that a kind of intermolecular distance is little, adhesive ability is strong
, may be used for macromolecule memory material of the close benefit of tire leakproof and preparation method thereof.Especially following some obtain prominent
Effect: 1, have employed the mode that high speed rotating is centrifugal, find which can be by macromolecule memory material through Experimental comparison
Molecule be centrifuged dispersion, the distance between reduction molecule, make macromolecule memory material reach nanoscale, and then improve it and inhale
Attached ability;
2, use vacuumizing and drying step, dry under vacuum conditions, can more preferable stable molecule spacing, it is ensured that
The absorbability of macromolecule memory material.
Above content is further description the most made for the present invention, it is impossible to assert the present invention
Be embodied as be confined to these explanations.For general technical staff of the technical field of the invention, without departing from
On the premise of present inventive concept, it is also possible to make some simple deduction or replace, all should be considered as belonging to the protection model of the present invention
Enclose.
Claims (3)
1. the preparation method of a macromolecule memory material, it is characterised in that comprise the steps:
Adhesive paste preparation process, by the pentalyn of 30 to 50 parts of weight, the terpene resin of 40 to 50 parts of weight, 10 to 20
Part diethyl phthalate of weight, the N of 2 to 5 parts of weight, N '-diphenyl-para-phenylene diamine, the hydroxide of 5 to 10 parts of weight
Aluminum, the nano-calcium carbonate of 5 to 10 parts of weight, 4,4 '-bis oxide benzene sulfur hydrazine of 1 to 5 part of weight and the N of 1 to 3 part of weight,
N-dimethyl ethylamino ethylene glycol is fully ground, and hydrolyzes under acid or alkaline conditions, adds 50 to 70 parts of weight
SEPS thermoplastic elastomer and the polyisoprene rubber of 40 to 50 parts of weight, be heated to more than its fusing point, mix and blend until
It is visible by naked eyes granule, it is thus achieved that adhesive paste;
High speed rotating centrifugation step, puts into centrifuge after described adhesive paste is cooled to room temperature, high speed rotating is centrifuged 90-120 minute,
Rotating speed is 25000 × g-30000 × g;
Vacuumizing and drying step, puts into process 35-in the vacuumizing and drying device that vacuum is 1 Pascal by the adhesive paste after centrifugal
55 minutes;
Curing schedule, takes out the adhesive paste after centrifugal drying, solidifies the sub-memory material that i.e. secures satisfactory grades for 24 hours at ambient temperature.
2. the preparation method of macromolecule memory material as claimed in claim 1, it is characterised in that
Adhesive paste preparation process, by the pentalyn of 43 parts of weight, the terpene resin of 47 parts of weight, the adjacent benzene of 16 parts of weight
Dicarboxylate, the N of 3 parts of weight, N '-diphenyl-para-phenylene diamine, the aluminium hydroxide of 7 parts of weight, the nano-sized carbon of 8 parts of weight
Acid calcium, 4,4 '-bis oxide benzene sulfur hydrazine of 2 parts of weight and the N of 2 parts of weight, N-dimethyl ethylamino ethylene glycol fully grind
Mill, and hydrolyze under acid or alkaline conditions, add the SEPS thermoplastic elastomer of 62 parts of weight and the poly-isoamyl of 45 parts of weight
Diene rubber, is heated to more than its fusing point, and mix and blend is until being visible by naked eyes granule, it is thus achieved that adhesive paste;
High speed rotating centrifugation step, puts into centrifuge after described adhesive paste is cooled to room temperature, high speed rotating is centrifuged 105 minutes, turns
Speed is 27500 × g;
Vacuumizing and drying step, puts into process 45 in the vacuumizing and drying device that vacuum is 1 Pascal by the adhesive paste after centrifugal
Minute;
Curing schedule, takes out the adhesive paste after centrifugal drying, solidifies the sub-memory material that i.e. secures satisfactory grades for 24 hours at ambient temperature.
3. a macromolecule memory material, it is characterised in that take the macromolecule memory as described in arbitrary in claim 1 or 2
The preparation method of material is made.
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CN103992765B true CN103992765B (en) | 2016-09-28 |
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Families Citing this family (4)
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CN106496681A (en) * | 2016-11-08 | 2017-03-15 | 湖南驰轩汽车服务有限公司 | The nano combined memory glue of tire and its using method |
US10865326B2 (en) | 2017-09-20 | 2020-12-15 | Ppg Industries Ohio, Inc. | Coating compositions, elastic barrier coatings formed therefrom, and methods of applying such coatings |
US10836924B2 (en) | 2019-03-15 | 2020-11-17 | Ppg Industries Ohio, Inc. | Coating compositions and elastic barrier coatings formed therefrom |
US10829664B2 (en) | 2019-03-15 | 2020-11-10 | Ppg Industries Ohio, Inc. | Coating compositions containing polythioethers and elastic barrier coatings formed therefrom |
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CN1935894A (en) * | 2005-09-21 | 2007-03-28 | 张海龙 | Polymer self-repair sealing material |
CN102634307A (en) * | 2012-05-03 | 2012-08-15 | 河南羚锐制药股份有限公司 | Hot-melting pressure sensitive adhesive and preparation method thereof |
CN103044841A (en) * | 2013-01-09 | 2013-04-17 | 无锡安睿驰科技有限公司 | Macromolecular synthesized memory sizing material |
CN103333649A (en) * | 2013-06-01 | 2013-10-02 | 黄山市休宁信德成化工有限公司 | Hot-melt and pressure sensitive plaster matrigel and preparation method thereof |
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2014
- 2014-06-10 CN CN201410254409.6A patent/CN103992765B/en active Active
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
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CN1935894A (en) * | 2005-09-21 | 2007-03-28 | 张海龙 | Polymer self-repair sealing material |
CN102634307A (en) * | 2012-05-03 | 2012-08-15 | 河南羚锐制药股份有限公司 | Hot-melting pressure sensitive adhesive and preparation method thereof |
CN103044841A (en) * | 2013-01-09 | 2013-04-17 | 无锡安睿驰科技有限公司 | Macromolecular synthesized memory sizing material |
CN103333649A (en) * | 2013-06-01 | 2013-10-02 | 黄山市休宁信德成化工有限公司 | Hot-melt and pressure sensitive plaster matrigel and preparation method thereof |
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Effective date of registration: 20190606 Address after: Room 1817, Liwan Building, 101 Qianhai Road, Nanshan Street, Shenzhen City, Guangdong Province Patentee after: Aerospace Dragon Technology (Shenzhen) Co., Ltd. Address before: 510000 Room 602, West Ladder, Fuhua Building, 377 Slender Dogling Road, Tianhe District, Guangzhou City, Guangdong Province Patentee before: Rao Xiuqin |